FAM61B Rabbit pAb, Biotin conjugated(bs-11001R-Bio)-100ul

FAM61B Rabbit pAb, Biotin conj

ugated(bs-11001R-Bio)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-11001R-Bio
  • 2025年09月30日
  • 产品信息以Bioss网站为准
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      100ul

    产品编号bs-11001R-Bio
    英文名称FAM61B Rabbit pAb, Biotin conjugated
    中文名称Biotin标记的FAM61B蛋白抗体
    英文别名Protein FAM61B; Putative uncharacterized protein C20orf40; LSM14 homolog B(SCD6, S. cerevisiae); bA11M20.3; C20orf40; Chromosome 20 open reading frame 40; Family with sequence similarity 61 member B; LSM13; LSM14 homolog B; LSM14B SCD6 homolog B(S. cerevisiae); MGC61931; Protein LSM14 homolog B; RNA associated protein 55B; LS14B_HUMAN; LSM14B; bA11M20.3; C20orf40; FAM61B; FT005; LSM13; RAP55B.
    产品应用Flow-Cyt=1ug/test

    Not yet tested in other applications.
    Optimal working dilutions must be determined by the end user.

    抗体来源Rabbit
    免疫原KLH conjugated synthetic peptide derived from human FAM61B
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    浓度1mg/ml
    储存液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    研究领域

    Cell Biology > Other Antibodies > Other Antibodies

    Epigenetics and Nuclear Signaling > DNA / RNA > Translation > Regulation

    亚基Component of a ribonucleoprotein (RNP) complex (By similarity).
    相似性Belongs to the LSM14 family. _x000D_
    Contains 1 DFDF domain. _x000D_
    功能May play a role in control of mRNA translation (By similarity). _x000D_
    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    背景资料Sm and Sm-like (LSm) proteins form donut-shaped, ubiquitously expressed heptameric complexes that are involved in various steps of RNA metabolism, including RNA-protein interactions and structural changes that are required during ribosomal subunit assembly. LSm14B, also known as C20orf40, FAM61B or LSM13, is a 385 amino acid protein that exists as multiple alternatively spliced isoforms and may play a role in RNA-related events. The gene encoding LSm14B maps to human chromosome 20. Comprising approximately 2% of the human genome, chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome.

     

    应用推荐稀释比例
    {Flow-Cyt}{1ug/test}

     

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